| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00042 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:1076780-1078110 |
Target genes | | Number: 55 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:1076864-1076884 | CCCCACCACATCCCCACCCC | + | 6.61 | | ZNF263 | MA0528.1 | chr1:1076840-1076861 | CCTTCCCCCGCCTCCACCCCC | - | 6.04 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_24482 | chr1:1077845-1081465 | Colon_Crypt_2 | | SE_24970 | chr1:1077814-1082618 | Colon_Crypt_3 | | SE_52392 | chr1:1077928-1081420 | Small_Intestine | | SE_56870 | chr1:1077148-1077618 | VACO_400 | | SE_56870 | chr1:1077851-1078401 | VACO_400 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1077843 | 1077954 | | chr1 | 1077898 | 1077977 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I001141 | chr1 | 1077149 | 1077618 | | GH01I001142 | chr1 | 1077792 | 1081590 |
|
Enhancer Sequence | TCCTTACCTC TATCCCCACC CACATCCTTA CCCCCATCCC CGCCCCGTCC ACAACCCCAT 60
CCTTCCCCCG CCTCCACCCC CCGCCCCCAC CACATCCCCA CCCCTGTCCC CACCCCTGTC 120
CCCACCCTCA TCCCCACCCC TGTCCCCCCC ATCCCTGCTT CCCCAACTGC ATCCACCTGA 180
CTCCCTCCTG TCCCCACCAA CCCGGCCAAG CGTCCTCCCT CTCAGAGGCT CTCGCTTGCC 240
CCCCACAGTG CCCCTCCAAC CCCCAGCCTC AATGAACGTC CCCCGGCCTG GCCTCCTGCA 300
CCCAGAGAGT GGCCTTCGGA GGCCGCAGCC GTCTCGCCCA CGGTCCCCGG TCCATGCTGC 360
TCCCTCCTCT CAGCTCCCCT CAGCCCGAGC CCCAGGAGAC AGGCACCTGG GCCCGTGGGC 420
CGACCGGGGG AGACCCTGCA TGGTTGTGGA TCCCTGGGGG CAGCTTCACG CTGGGCTTTG 480
GTCCCCAGGG CCCAAGACCA CTCCCCTACC CTCGGCTCCA CAGCTGACCT GGCTACAGGA 540
AACACCGGCC CCTCTTTGGC TTCTGAAGAC CCCACAGGCT CTTGCCACCC CCGCCTGCCT 600
CCTCCTCACG TCAACCCGTC AGTCCTCGGC GTGGACGCTG TCCTCAGGAG AGGGGAGCCC 660
CCAGGCCTGG ACCCCTCTGT GCTCGGGAGA GGGGAGCCCC CAGGCCTGGA CCCCTCTGTG 720
CTCGGGAGAG GGGAGCCCCC AGGCCTGGAC CCCTCGGCTG GGGCCCTGCG CTCCCACTGA 780
GCCGTGTCTG CCCTCAGTCC CCAGCACACC ATCCCCGTCT CTCTTTTTTT TTATTTTTTC 840
GAGATGAAGT CTTGCTCTGT CACCCAGGCT AGAGTGCAGT GGCACGATCT CGGCTCACTG 900
CAACCTCCAC CTCCCGGGTT CAAGGGATTC TCCTGCCTCA GCCCCTGAGT AGTTGGGATT 960
ACAGGTGCCC AGCATCACAC CCGGCTAATT TTTGTATTTT TAGTAGAGAT GGGGCTTCAC 1020
CATGTTGGCC AGGCTGGTCT CAAACTCCTG ACCTCAAATG ATCCGCCCAC CTCGGCCTCC 1080
CACAGTGCTG GGATTACAGG CGTGAGTCAC TGTGCCCGAC CCCGTCCCCG TCTTTCAGTC 1140
AAGACCGTCC TCCCCACAGC ACCCCTGCAC TGCCGCCCTC TCAGCCTCCC GTTTAGCAAA 1200
ACGGTTCCCC CACTGCCTCC TGCCACGACC CCAGCCTCCC CTCGGCCTCT GAAGGCAGCC 1260
GGGACCCCTG CTGTCCTCCC ACCTCCCCAC CTGCACGCTC TGCTCCTCCT ACCTTCTAAA 1320
AGGATCTTCC 1330
|
